2001
DOI: 10.1046/j.1365-2222.2001.01122.x
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Allergen‐induced basophil activation: CD63 cell expression detected by flow cytometry in patients allergic to Dermatophagoides pteronyssinus and Lolium perenne

Abstract: The basophil activation test is a highly reliable technique in the diagnosis of allergy to inhalant allergens. The sensitivity of the basophil activation test was 93.3%, and its specificity 98.4%, when using a cut-off point of 15% activated basophils as positive result.

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Cited by 100 publications
(108 citation statements)
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“…Flow cytometric analysis of in vitro activated basophils using CD63 neo-expression has proved quite reliable for the diagnosis of different IgE-mediated allergies including allergies to inhalant allergens (e.g. pollen allergy) [10], food [2] and venom [3]. It has also been used with some success in evaluating reactions to drugs, including muscle relaxants.…”
Section: Discussionmentioning
confidence: 99%
“…Flow cytometric analysis of in vitro activated basophils using CD63 neo-expression has proved quite reliable for the diagnosis of different IgE-mediated allergies including allergies to inhalant allergens (e.g. pollen allergy) [10], food [2] and venom [3]. It has also been used with some success in evaluating reactions to drugs, including muscle relaxants.…”
Section: Discussionmentioning
confidence: 99%
“…Specific IgE blood testing may be preferred by primary care physicians because testing is relatively ease to manage and results are highly accurate [24 -28]. Another test, the basophil activation test is also a highly reliable technique in the diagnosis of allergy to inhalant allergens [29]. Findings from other studies; however, posit that specific IgE blood levels may not be consistent if a patient is followed using 2 different assay systems [30].…”
Section: Discussionmentioning
confidence: 99%
“…In vitro challenge of basophils with Gelofusine All participants underwent the BAT with Gelofusine, employing a technique using whole blood samples modified from that described by Sanz et al [12]. Heparinised blood (100 ll) was incubated with 20 ll stimulation buffer containing 2 ng.ml ; Sigma) was added to each tube and flow cytometric analysis performed using a FACScalibur flow cytometer and CELL QUEST software (BD Biosciences, San Jose, CA).…”
Section: Methodsmentioning
confidence: 99%